rs151246531
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
G
Chromosome
10
Location
78037292
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.378T>G (p.Gly126=)
Allele
G
Clinical Significance
Benign